Variant report

Variant	rs10989605
Chromosome Location	chr9:104486668-104486669
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10512283	0.92[ASN][1000 genomes]
rs10512284	0.92[ASN][1000 genomes]
rs10512286	0.92[ASN][1000 genomes]
rs10819954	0.92[ASN][1000 genomes]
rs10819955	0.92[ASN][1000 genomes]
rs10819956	0.92[ASN][1000 genomes]
rs10819958	0.92[ASN][1000 genomes]
rs10819959	0.92[ASN][1000 genomes]
rs10819961	0.92[ASN][1000 genomes]
rs10819977	0.92[ASN][1000 genomes]
rs10989572	0.92[ASN][1000 genomes]
rs10989592	0.92[ASN][1000 genomes]
rs10989594	0.92[ASN][1000 genomes]
rs10989596	0.92[ASN][1000 genomes]
rs10989597	0.92[ASN][1000 genomes]
rs10989598	0.92[ASN][1000 genomes]
rs12338602	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12708308	0.92[ASN][1000 genomes]
rs1323427	0.92[ASN][1000 genomes]
rs13289501	0.92[ASN][1000 genomes]
rs1337684	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1407873	0.92[ASN][1000 genomes]
rs1407874	0.92[ASN][1000 genomes]
rs17197124	0.92[ASN][1000 genomes]
rs17199066	0.92[ASN][1000 genomes]
rs1853447	0.92[ASN][1000 genomes]
rs2225879	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2417291	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28653415	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34360878	0.92[ASN][1000 genomes]
rs34888126	0.84[ASN][1000 genomes]
rs35227408	0.92[ASN][1000 genomes]
rs35569161	0.84[ASN][1000 genomes]
rs35958820	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4266702	0.92[ASN][1000 genomes]
rs4442195	0.92[ASN][1000 genomes]
rs4743484	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55749212	0.84[ASN][1000 genomes]
rs56052939	0.84[ASN][1000 genomes]
rs6479060	0.92[ASN][1000 genomes]
rs72745355	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1046590	chr9:104450624-104848588	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104480800-104491400	Weak transcription	Liver	Liver

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